Primary Site >> Stomach Cancer

Gene >> PDYN

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000217305
Start 1983032:1983032(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.53C>T
AA Mutation p.Thr18Ile(p.T18I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000217305
Start 1980406:1980406(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763424462
CDS Mutation c.682G>A
AA Mutation p.Gly228Ser(p.G228S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000217305
Start 1980453:1980453(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138498390
CDS Mutation c.635G>A
AA Mutation p.Arg212Gln(p.R212Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000217305
Start 1980394:1980394(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376562868
CDS Mutation c.694C>T
AA Mutation p.Arg232Cys(p.R232C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000217305
Start 1980468:1980468(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.620A>T
AA Mutation p.Tyr207Phe(p.Y207F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000217305
Start 1980546:1980546(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.542A>G
AA Mutation p.Lys181Arg(p.K181R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000217305
Start 1980631:1980631(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.457G>A
AA Mutation p.Asp153Asn(p.D153N)
Mutation Classification Missense_Mutation
Feature Type Transcript